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Journal Abstract Search

117 related items for PubMed ID: 21551967

  • 1. A 6-year-old girl with hemoglobin H disease.
    Ueda T, Migita M, Yamanishi M, Maeda M, Harano K, Fukunaga Y.
    J Nippon Med Sch; 2011; 78(2):101-4. PubMed ID: 21551967
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  • 2. Identification of one or two α-globin gene deletions by isoelectric focusing electrophoresis.
    Agarwal AM, Nussenzveig RH, Hoke C, Lorey TS, Greene DN.
    Am J Clin Pathol; 2013 Sep; 140(3):301-5. PubMed ID: 23955447
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  • 3. A novel α(0) -thalassemia deletion in a Greek patient with HbH disease and β-thalassemia trait.
    Phylipsen M, Traeger-Synodinos J, van der Kraan M, van Delft P, Bakker G, Geerts M, Kanavakis E, Stamoulakatou A, Karagiorga M, Giordano PC, Harteveld CL.
    Eur J Haematol; 2012 Apr; 88(4):356-62. PubMed ID: 22324317
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  • 9. [A Japanese family with hereditary HbH disease--a case report and its gene analysis].
    Hattori Y, Yamashiro Y, Yamamoto K, Morishita M, Miyaji T, Yamamoto K, Matsuno Y, Fujii H, Miwa S, Ichimaru M.
    Rinsho Ketsueki; 1990 Feb; 31(2):183-8. PubMed ID: 2329681
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  • 20. Disease burden, management strategies, and unmet needs in α-thalassemia due to hemoglobin H disease.
    Lal A, Viprakasit V, Vichinsky E, Lai Y, Lu MY, Kattamis A.
    Am J Hematol; 2024 Nov; 99(11):2164-2177. PubMed ID: 39037279
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